SCHEMBL9040401

SCHEMBL9040401

CC(=O)c1c(F)c(F)c(O)c(F)c1F

nearest known ligand 0.44

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
ESR1 P03372 1/20 0.44
CYP3A4 P08684 3/20 0.39
THRB P10828 1/20 0.39
MEN1 O00255 1/20 0.39
HPGD P15428 1/20 0.39
KMT2A Q03164 1/20 0.39
SMN1; SMN2 Q16637 2/20 0.32
ALDH1A1 P00352 1/20 0.32
MAPK1 P28482 1/20 0.32
NPSR1 Q6W5P4 1/20 0.32
PRKCI P41743 1/20 0.32
CES2 O00748 1/20 0.32
CES1 P23141 1/20 0.32
PTGES O14684 1/20 0.31
ALOX5 P09917 1/20 0.31
CA12 O43570 1/20 0.31
CA9 Q16790 1/20 0.31
PKM P14618 1/20 0.30
L3MBTL1 Q9Y468 1/20 0.30
CYP1A2 P05177 1/20 0.30

Click a target to see other patent compounds predicted against it — the reverse direction, in place.

Similar compounds — the chemically nearest patent molecules

Nearest neighbours by Morgan-fingerprint cosine across the patent-compound collection, with each neighbour's top predicted target and the predicted targets it shares with this molecule.

Compoundsimilaritytop predictedshared targets
SCHEMBL9377547 0.90 ESR1 (0.41) ESR1CYP3A4THRBMEN1HPGD
SCHEMBL823811 0.85 CES2 (0.42) CYP3A4THRBMEN1HPGDKMT2A
SCHEMBL19360080 0.85 CES2 (0.42) CYP3A4THRBMEN1HPGDKMT2A
SCHEMBL29042640 0.82 CYP3A4 (0.39) CYP3A4THRBMEN1HPGDKMT2A
SCHEMBL31403419 0.80 CYP3A4 (0.35) CYP3A4THRBMEN1HPGDKMT2A
Acetic Acid SCHEMBL9135699 0.79 FFAR3 (0.47) ESR1
SCHEMBL124392 0.79 CES2 (0.42) CYP3A4THRBMEN1HPGDKMT2A
SCHEMBL10174835 0.78 MEN1 (0.37) CYP3A4THRBMEN1HPGDKMT2A
SCHEMBL6727338 0.78 TAS1R3 (0.47) CYP3A4THRBKMT2ACYP1A2
Acetic Acid SCHEMBL3565472 0.77 FFAR3 (0.44) ESR1

Similarity is cosine over the 2,048-bit Morgan fingerprint (≈ Tanimoto). Identical fingerprints score 1.00.

Patent provenance — the patents this molecule appears in, and who filed them

Claimed or disclosed in 6 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20220157484-A1 POLYURETHANE, POLYURETHANE PRODUCTION METHOD, CONDUCTIVE PASTE COMPOSITION, CONDUCTIVE WIRE, AND METHOD FOR PRODUCING CONDUCTIVE WIRE SHIN-ETSU CHEMICAL CO., LTD. (JP) 2022-05-19 US disclosed
US-8299055-B2 8-substituted isoquinoline derivative and the use thereof ASAHI KASEI PHARMA CORPORATION (JP) 2012-10-30 US disclosed
US-20100261701-A1 8-Substituted isoquinoline derivative and the use thereof ASAHI KASEI PHARMA CORPORATION (JP) 2010-10-14 US disclosed
EP-0512352-B1 Substituted carboxylic acid derivatives HOFFMANN LA ROCHE (CH) 1996-03-27 EP disclosed
US-5344843-A Carnitine acryltransferase enzyme inhibitors as antiischemic agents and for cardiovascular disorders HOFFMAN-LA ROCHE INC. (US) 1994-09-06 US disclosed
EP-0512352-A2 Substituted carboxylic acid derivatives F. HOFFMANN-LA ROCHE AG (CH) 1992-11-11 EP disclosed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (1 of them — usually the abstract, not the full specification), we ask MedCPT which protein the text reads most about, and where the chemistry-predicted target lands among 4885 human targets. A high rank means the patent's own wording is consistent with the prediction — a weak, independent signal, not proof of activity.

PatentTitleText reads most aboutPredicted target · text-rank
US-20100261701-A1 8-Substituted isoquinoline derivative and the use thereof RELA, NFKBIA, NFKB2 ESR1 2004/4885CYP3A4 4163/4885THRB 2005/4885

“Text reads most about” is the patent abstract's nearest protein in MedCPT space (background-debiased). Only ~1.4% of patents have machine-readable text, so most compounds won't have this panel.